)Kontinuierliche Überwachung sowie Reporting der Verkaufs-, Markt- und Wettbewerbszahlen, inklusive Adaptieren der entsprechenden AktivitätenÜbernahme und Support administrativer Aufgaben. Für diese Position
Für unseren Value Stream – Site Logistics Support in Marburg suchen wir aktuell eine/n Teamleiter/in Support (m/w/x) R-249579 Vollzeit / unbefristet Aufgaben Personaleinsatzplanung
Für unseren Value Stream – Site Logistics Support in Marburg suchen wir aktuell eine/n Teamleiter/in Support (m/w/x) R-249578 Vollzeit / unbefristet Aufgaben Personaleinsatzplanung
support Seqirus. You will partner with commercial heads and ensures alignment on key strategies, deliverables & communication. You will serve as Influenza and other vaccines champion/expert
groundbreaking innovations worldwide. Through our research, we support the development of effective and safe medical agents to help improve the cures for diseases such as cancer. We have been growing steadily
, Sartocheck-Testgeräte) gemäß Anforderungen aus der ProduktionInstallation von neuer Hard- und SoftwareSchulung der Benutzer im MESNeuanlage und Pflege von User Accounts im MESSecond Level Support für die MES
updates of the Global Value Dossier, supporting affiliate P&R and HTA submissions.Support Country Teams: Provide guidance and support to country teams during P&R and HTA submissions, negotiations, and
great job opportunity will be located in Marburg and reports directly into the Associate Director Services and Consultancy Sourcing in Australia. The Opportunity In this position you will support
. The Role Lead and manage a team of event and contract administration specialists.Define goals and objectives with team members to achieve short-term operational results.Provide guidance and support
for New Product OpportunitiesUtilise insights from the product development pathway and global biopharmaceutical trends to guide R&D policy, support preparation of regulator packages and identify new
and develop a team comprised of process engineers and or scientistLead technical workstreams of complex projects at the site level or at the global level to support process changes, process improvements
groundbreaking innovations worldwide. Through our research, we support the development of effective and safe medical agents to help improve the cures for diseases such as cancer. We have been growing steadily
As a Drug Product (DP) External Manufacturing Lead you will be responsible for providing process engineering support for all DP manufacturing conducted on behalf of CSL Behring Operations at contract
external collaborators to make recommendations on study design, execution and data analysis. The Role Oversee and provide support in statistical methodology for experimental design, data analysis
Fulltime / permanent/ non-tariff Do you want to work in a global team and support regulatory strategies of plasma-derived products in all phases of development, from preclinical to post approval phase
primary point of contact for all Omnichannel-related inquiries across the DACH region and act as a business partner to support the business units in implementing their strategies. (strong implementation
customer service and operational specialists.Define goals and objectives with team members to achieve short-term operational results.Provide guidance and support to team members to ensure their
: direct communication with doctors and pharmacists as well as print, TV and digital marketing. To further expand our rapidly growing business, we are looking for a Head of Asia (f/m/d) to support us in this
: direct communication with doctors and pharmacists as well as print, TV and digital marketing. To further expand our rapidly growing business, we are looking for a Head of US (f/m/d) to support us in this
Job Overview: As Associate Director, you will liaise with cross-functional teams, to drive the quality statistical planning, analysis and reporting in support of pharmaceutical development and
support statistical programming activities related to the analysis of real-world data. This role involves working closely with biostatisticians, epidemiologists, clinical scientists, medical affairs, health
. The main responsibilities of the role are: Industrial Relations Support Industrial Relations queries across the CSL group by partnering with partners to provide professional, and accurate advice
patients.Develop clinical trial supply documents and training to support study execution for clinical sites and patients (e.g. Investigational Medicinal Product (IMP) Manuals, product preparation and administration
designated cluster. This position provides expert input on pharmacovigilance-related matters and develops strategy for the assigned cluster, ensuring PV processes are completed seamlessly in support of the
training to support study execution for clinical sites and patients (e.g. Investigational Medicinal Product (IMP) Manuals, product preparation and administration videos). Trains external stakeholders (i.e
accumulated overtime for sabbaticals, special leave, or an early start into retirement (Marburg)Family services such as psychological support, legal advice, family care services and more for you and your direct
standards of patient safety and product efficacy. Today, we are setting new standards in digital urology to provide holistic care to patients seeking treatment and support the community on their road to
, Research & Development Quality Assurance (R&DQA) and Clinical.Maintains up-to-date understanding of safety profiles of registered and investigational products. Supports and collaborates with cross-functional
our customers from the pharmaceutical industry in Duisburg, Düsseldorf or Münster for direct recruitment. A fair compensation and personal support are of course included. You possess excellent